CAS 41398-85-0
:5-methylpyrimidin-2(1H)-one
Description:
5-Methylpyrimidin-2(1H)-one, also known as 5-methyl-2-pyrimidinone, is a heterocyclic organic compound characterized by a pyrimidine ring with a methyl group at the 5-position and a carbonyl group at the 2-position. This compound features a nitrogen-containing six-membered ring, which contributes to its basicity and potential reactivity in various chemical reactions. It is typically a white to off-white crystalline solid, soluble in polar solvents such as water and alcohols, due to the presence of the carbonyl group. The compound is of interest in medicinal chemistry and biochemistry, as it may serve as a building block for the synthesis of pharmaceuticals or as an intermediate in the preparation of other nitrogen-containing compounds. Its structure allows for potential interactions with biological systems, making it a candidate for further research in drug development. Safety data should be consulted for handling and storage, as with any chemical substance.
Formula:C5H6N2O
InChI:InChI=1/C5H6N2O/c1-4-2-6-5(8)7-3-4/h2-3H,1H3,(H,6,7,8)
SMILES:Cc1cnc(nc1)O
Synonyms:- 2(1H)-pyrimidinone, 5-methyl-
- 2-Pyrimidinol, 5-Methyl-
- 5-Methyl-2(1H)-pyrimidinone
- 2-Hydroxy-5-methylpyrimidine
- 5-Methylpyrimidin-2(1H)-one
- 5-Methyl-2-pyrimidinol hydrochloride
- 5-methyl-1H-pyrimidin-2-one
- 5-methyl-2-pyrimidinol
- 2(1H)-Pyrimidinone, 5-methyl- (7CI,9CI)
- 2-Hydroxy-5-methylpyrimidine ISO 9001:2015 REACH
- 5-methylpyrimidin-2-ol
- 5-methyl-2-pyrimidinone
- 5-Methylpyrimidin-2-ol hydrochloride
- See more synonyms
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Found 4 products.
2-Hydroxy-5-methylpyrimidine
CAS:Formula:C5H6N2OPurity:98%Color and Shape:SolidMolecular weight:110.11395-Methylpyrimidin-2-ol
CAS:5-Methylpyrimidin-2-olFormula:C5H6N2OPurity:≥95%Color and Shape: faint orange/red crystalline powderMolecular weight:110.11g/mol5-Methylpyrimidin-2-ol
CAS:<p>5-Methylpyrimidin-2-ol is a photophysical, hydroxy group, and hydroxyl group. It has been shown to have an inhibitory effect on DNA methylation by glycosidic bond with the sugar moiety of the nucleotide. 5-Methylpyrimidin-2-ol reacts with the base moiety of the nucleotide to form an analog that inhibits RNA synthesis and is competitive against pyrimidine nucleosides. 5-Methylpyrimidin-2-ol also has a hydrogen bonding property that can react with other molecules such as proteins or sugars to form hydrogen bonds. This reaction rate is increased by fluorescence resonance energy transfer (FRET).</p>Formula:C5H6N2OPurity:Min. 95%Color and Shape:PowderMolecular weight:110.11 g/mol



